FDA Adverse Event Injury Summary report: N

PRO-TEC

MDR report key: 518060 · Received March 26, 2004

Report

Report Number
1832816-2004-00001
Event Type
Injury
Date Received
March 26, 2004
Date of Event
February 6, 2004
Report Date
March 22, 2004
Manufacturer
STC PLASTICS, INC.
Product Code
MMK
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE PT WAS CLOSING THE LID ON THE SHARPS CONTAINER, FORCING THE LID CLOSED, AS THE CONTAINER WAS FULL. WHEN PT PICKED THE CONTAINER UP, PT WAS STUCK BY A NEEDLE.

Description of Event or Problem · 1

THE PT WAS CLOSING THE LID ON THE SHARPS CONTAINER, FORCING THE LID CLOSED, AS THE CONTAINER WAS FULL. WHEN THEY PICKED THE CONTAINER UP, THEY WERE STUCK BY A NEEDLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PRO-TEC SHARPS CONTAINER SAFETY SYSTEM MMK STC PLASTICS, INC. UNK S271745

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Required Intervention